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Aging selectively dampens oscillation of lipid abundance in white and brown adipose tissue

Lipid metabolism is under the control of the circadian system and circadian dysregulation has been linked to obesity and dyslipidemia. These factors and outcomes have also been associated to, or affected by, the process of aging. Here, we investigated whether murine white (WAT) and brown (BAT) adipo...

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Autores principales: Held, Ntsiki M., Buijink, M. Renate, Elfrink, Hyung L., Kooijman, Sander, Janssens, Georges E., Luyf, Angela C. M., Pras-Raves, Mia L., Vaz, Frédéric M., Michel, Stephan, Houtkooper, Riekelt H., van Weeghel, Michel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7961067/
https://www.ncbi.nlm.nih.gov/pubmed/33723320
http://dx.doi.org/10.1038/s41598-021-85455-4
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author Held, Ntsiki M.
Buijink, M. Renate
Elfrink, Hyung L.
Kooijman, Sander
Janssens, Georges E.
Luyf, Angela C. M.
Pras-Raves, Mia L.
Vaz, Frédéric M.
Michel, Stephan
Houtkooper, Riekelt H.
van Weeghel, Michel
author_facet Held, Ntsiki M.
Buijink, M. Renate
Elfrink, Hyung L.
Kooijman, Sander
Janssens, Georges E.
Luyf, Angela C. M.
Pras-Raves, Mia L.
Vaz, Frédéric M.
Michel, Stephan
Houtkooper, Riekelt H.
van Weeghel, Michel
author_sort Held, Ntsiki M.
collection PubMed
description Lipid metabolism is under the control of the circadian system and circadian dysregulation has been linked to obesity and dyslipidemia. These factors and outcomes have also been associated to, or affected by, the process of aging. Here, we investigated whether murine white (WAT) and brown (BAT) adipose tissue lipids exhibit rhythmicity and if this is affected by aging. To this end, we have measured the 24 h lipid profiles of WAT and BAT using a global lipidomics analysis of > 1100 lipids. We observed rhythmicity in nearly all lipid classes including glycerolipids, glycerophospholipids, sterol lipids and sphingolipids. Overall, ~ 22% of the analyzed lipids were considered rhythmic in WAT and BAT. Despite a general accumulation of lipids upon aging the fraction of oscillating lipids decreased in both tissues to 14% and 18%, respectively. Diurnal profiles of lipids in BAT appeared to depend on the lipid acyl chain length and this specific regulation was lost in aged mice. Our study revealed how aging affects the rhythmicity of lipid metabolism and could contribute to the quest for targets that improve diurnal lipid homeostasis to maintain cardiometabolic health during aging.
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spelling pubmed-79610672021-03-19 Aging selectively dampens oscillation of lipid abundance in white and brown adipose tissue Held, Ntsiki M. Buijink, M. Renate Elfrink, Hyung L. Kooijman, Sander Janssens, Georges E. Luyf, Angela C. M. Pras-Raves, Mia L. Vaz, Frédéric M. Michel, Stephan Houtkooper, Riekelt H. van Weeghel, Michel Sci Rep Article Lipid metabolism is under the control of the circadian system and circadian dysregulation has been linked to obesity and dyslipidemia. These factors and outcomes have also been associated to, or affected by, the process of aging. Here, we investigated whether murine white (WAT) and brown (BAT) adipose tissue lipids exhibit rhythmicity and if this is affected by aging. To this end, we have measured the 24 h lipid profiles of WAT and BAT using a global lipidomics analysis of > 1100 lipids. We observed rhythmicity in nearly all lipid classes including glycerolipids, glycerophospholipids, sterol lipids and sphingolipids. Overall, ~ 22% of the analyzed lipids were considered rhythmic in WAT and BAT. Despite a general accumulation of lipids upon aging the fraction of oscillating lipids decreased in both tissues to 14% and 18%, respectively. Diurnal profiles of lipids in BAT appeared to depend on the lipid acyl chain length and this specific regulation was lost in aged mice. Our study revealed how aging affects the rhythmicity of lipid metabolism and could contribute to the quest for targets that improve diurnal lipid homeostasis to maintain cardiometabolic health during aging. Nature Publishing Group UK 2021-03-15 /pmc/articles/PMC7961067/ /pubmed/33723320 http://dx.doi.org/10.1038/s41598-021-85455-4 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Held, Ntsiki M.
Buijink, M. Renate
Elfrink, Hyung L.
Kooijman, Sander
Janssens, Georges E.
Luyf, Angela C. M.
Pras-Raves, Mia L.
Vaz, Frédéric M.
Michel, Stephan
Houtkooper, Riekelt H.
van Weeghel, Michel
Aging selectively dampens oscillation of lipid abundance in white and brown adipose tissue
title Aging selectively dampens oscillation of lipid abundance in white and brown adipose tissue
title_full Aging selectively dampens oscillation of lipid abundance in white and brown adipose tissue
title_fullStr Aging selectively dampens oscillation of lipid abundance in white and brown adipose tissue
title_full_unstemmed Aging selectively dampens oscillation of lipid abundance in white and brown adipose tissue
title_short Aging selectively dampens oscillation of lipid abundance in white and brown adipose tissue
title_sort aging selectively dampens oscillation of lipid abundance in white and brown adipose tissue
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7961067/
https://www.ncbi.nlm.nih.gov/pubmed/33723320
http://dx.doi.org/10.1038/s41598-021-85455-4
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